Senior qc analyst Work, Jobs in Guildford, Sry (with Salaries)

Senior QC Analyst
Nelsons —London
- Full-time
- Laboratory experience
- Supervising experience
- Quality control
- Employee discount
Quick apply
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- Doctoral degree
- Master's degree
- Communication skills

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Senior QC Analyst

Nelsons -
London

Quick apply

Job details

Full-time

Benefits

Cycle to work scheme
Employee discount

Qualifications

Report writing
GLP
Non-conformance investigation
Quality control sampling and lab testing
Report generation
Analytical chemistry
Laboratory housekeeping
Laboratory experience
ERP software
Quality control within general manufacturing industry
Internal department liaison
Supervising experience
Quality control
Data entry
Training & development
Business coaching
Instrumentation calibration

Full job description

Nelsons is the UK’s largest manufacturer of natural healthcare products, operating in the market place for over 150 years with a wide range of brands and products; inspiring generations to live healthier and happier lives. We are proud of our brands - RESCUE range, Bach Original Flower Remedies, Spatone, Nelsons Arnicare, Nelsons Teetha, Nelsons creams including Calendula – which are distributed worldwide to over 60 countries.

Purpose

Participation as an active and flexible Quality department team member to provide Quality Control services for the Endeavour Supply Chain Organisation and Spatone production operations. To provide training and support to all other analysts and to support the QC Manager in the daily Quality Control demands from production which include sampling and testing of raw material & finished product, support to the validation team, the provision of accurate, approved data to the Quality Assurance team for review and ensure adherence to Good Laboratory Practices within the laboratory.

Responsibilities:

Ensure all training relevant to the position and required tasks are completed and kept up to date. Use assigned initials within cGMP environment.
All documentation relating to Nelson’s products are kept within Quality Management System (QMS) and adhere to Data Integrity (see POL-002).
Understanding and adhering to cGMP environment requirements.
Assist with the review and management of all QC Processes
Ensure timely sampling and testing of all raw materials, packaging components and finished product according to specification.
Assist with the daily management of all QC Processes including Q-Pulse training/Q-Pulse action adherence for the QC department.
The management of Q-Pulse asset module ensuring equipment is qualified, validated and the scheduling of all calibration activities.
Manage the review of QC SOP/WI in a timely manner.
Assist with the ongoing training to all analysts in laboratory methods.
Approve analysis worksheets performed by QC Analysts.
Sample and test all incoming raw materials, bulk and finished products.
Regular review and application of all applicable pharmacopeia methods and updates.
Ensure that all Out of Specification (OOS) results are reported and investigated via the correct procedures
Perform analysis, examination or investigations as required on behalf of the company.
Supply written reports as necessary on request
Assist the validation team with Method Transfer, Process & Equipment validation projects within the laboratory.
Ensure all data is stored and entered in the correct file.
Contribute to the investigation of customer complaints as required
Ensure the laboratory is maintained in a clean and tidy condition, including the removal of laboratory waste
Ensure all retained samples are kept and stored correctly.
Liaise effectively with staff from other departments
Involvement in other QMS responsibilities as required
Develop objectives and personal development plans with direct reports.

Requirements

We would love you to have

Education / Qualifications Degree level or above in a Science subject

Supervisor experience in an analytical laboratory role
Experience in analytical test method development and validation
Experience in conducting Out of Specification (OOS) Investigations
Ability to plan and prioritise work accordingly to production needs
Hands on/Active team member assisting with coaching of peers
Ability to use work instructions and specifications for testing of products and raw materials
A good interpretation & practical knowledge of Good Manufacturing Practices (GMP) & Good Laboratory Practice (GLP)
Strong report writing skills
A good level of wet bench chemistry skills
Good Attention to detail
Practical and organised approach
Experience or knowledge of High-Performance Liquid Chromatography (HPLC) and Gas Chromatograph (GC) techniques
Experience of working in a regulated laboratory environment.

Bonus if you have

Experience in the use of pharmacopeia’s or knowledge of TLC techniques
Knowledge of ERP systems such as SAP
Experience of pharmaceutical production processes for tablets, liquids and creams
Basic knowledge of microbiology

Benefits

Annual bonus

25 days holiday per year PLUS Christmas shut down - whoop!

Free products and staff discounts to keep you healthy and happy

✨ Paid days off to volunteer for some awesome charities

Cycle to work scheme

We also have regular socials plus all your standard stuff such as pensions, eye test vouchers and season ticket loans. We can tell you all about what is available to you when you start!

Quick apply

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senior qc analyst jobs in guildford, sry

Senior QC Analyst

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